Management of complex approval projects for finished medicinal products between Asian manufacturers and customers in Latin America
Review and adaptation of technical supplier documentation for finished products and adaptation to the specific requirements in Latin America
Managing the entire document flow for new approvals and existing products
Daily follow-ups and direct communication with the customer's regulatory affairs managers and suppliers
Professional preparation of supplier dossier content for the regulatory standards of the target markets
Management of GMP, quality and product documentation
Close cooperation with the CEO and the internal sales managers
Your profile
Scientific studies (pharmacy) or comparable training
Several years of experience in regulatory affairs, ideally in an international trading environment
Confident communication in business fluent English and Spanish (verbal and written)
Structured way of working with the ability to coordinate complex projects across multiple time zones
Enjoyment of international contacts
Team player who appreciates an independent way of working in a small but excellent team
Your benefits
A future-oriented, very interesting and lively position
Appreciative, collegial cooperation in a family environment with a flat hierarchy
A modern working environment in the city of Basel
Our customer
Rhenochem AG, based in the heart of Basel, is part of the Rhenopharma Group (www.rhenopharma.com) and is very successful in the global distribution of medicines for the pharmaceutical industry. Over the years, Rhenochem AG has developed into a specialist with strong technical expertise in the LATAM market. The name Rhenochem is well established in the trade of customer-specific finished products, classic active ingredients and innovative project services. In order to guarantee customers and suppliers services of the highest standard in the future, the following position is being created.
